Canonical Allele Identifier: CA3085548411

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26460094C= , CM000664.2:g.26460094C=	GRCh38
NC_000002.11:g.26682962C= , CM000664.1:g.26682962C=	GRCh37
NC_000002.10:g.26536466C=	NCBI36
NG_009937.1:g.103605G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.5925G= MANE Select	ENSP00000272371.2:p.Leu1975=
ENST00000339598.8:c.3512+553G= MANE Plus Clinical	ENSP00000344521.3:n.3512+553G=
ENST00000402415.8:c.3684G=	ENSP00000383906.4:p.Leu1228=
ENST00000272371.6:c.5925G=	ENSP00000272371.2:p.Leu1975=
ENST00000338581.10:c.3624G=	ENSP00000345137.6:p.Leu1208=
ENST00000339598.7:c.3512+553G=	ENSP00000344521.3:n.3512+553G=
ENST00000402415.7:c.3855G=	ENSP00000383906.3:p.Leu1285=
ENST00000403946.7:c.5813+553G=	ENSP00000385255.3:n.5813+553G=
NM_001287489.1:c.5813+553G=	NP_001274418.1:n.5813+553G=
NM_004802.3:c.3624G=	NP_004793.2:p.Leu1208=
NM_194248.2:c.5925G=	NP_919224.1:p.Leu1975=
NM_194322.2:c.3855G=	NP_919303.1:p.Leu1285=
NM_194323.2:c.3512+553G=	NP_919304.1:n.3512+553G=
XM_005264644.2:c.5798+553G=	XP_005264701.1:n.5798+553G=
XM_011533185.1:c.5858+553G=	XP_011531487.1:n.5858+553G=
XM_017005338.1:c.5865G=	XP_016860827.1:p.Leu1955=
NM_001287489.2:c.5813+553G=	NP_001274418.1:n.5813+553G=
NM_004802.4:c.3624G=	NP_004793.2:p.Leu1208=
NM_194248.3:c.5925G= MANE Select	NP_919224.1:p.Leu1975=
NM_194322.3:c.3855G=	NP_919303.1:p.Leu1285=
NM_194323.3:c.3512+553G= MANE Plus Clinical	NP_919304.1:n.3512+553G=